Compounds

Abstract

The present invention relates to compounds of formula (I): comprising a 5-membered nitrogen-containing heteroaryl ring A, wherein the heteroaryl ring A is substituted with at least one group containing an oxygen atom, and wherein said oxygen atom is attached to the heteroaryl ring A via at least two other atoms. The present invention further relates to salts, solvates and prodrugs of such compounds, to pharmaceutical compositions comprising such compounds, and to the use of such compounds in the treatment and prevention of medical disorders and diseases, most especially by the inhibition of NLRP3.

The invention claimed is: 
     
       1. A compound of formula (I): 
       
         
           
           
               
               
           
         
         or a pharmaceutically acceptable salt or solvate thereof, wherein:
 ring A is monocyclic; 
 Q is selected from O or S; 
 V is selected from N or C, and W, X, Y and Z are each independently selected from N, O, NH or CH, wherein at least one of V, W, X, Y and Z is N or NH; 
 L is a saturated or unsaturated hydrocarbylene group, wherein the hydrocarbylene group may be straight-chained or branched, or be or include cyclic groups, wherein the hydrocarbylene group may optionally be substituted, and wherein the hydrocarbylene group may optionally include one or more heteroatoms N, O or S in its carbon skeleton; 
 R 1  is hydrogen or a saturated or unsaturated hydrocarbyl group, wherein the hydrocarbyl group may be straight-chained or branched, or be or include cyclic groups, wherein the hydrocarbyl group may optionally be substituted, and wherein the hydrocarbyl group may optionally include one or more heteroatoms N, O or S in its carbon skeleton; 
 optionally L and R 1  together with the oxygen atom to which they are attached may form a 3- to 12-membered saturated or unsaturated cyclic group, wherein the cyclic group may optionally be substituted; 
 R 2  is a cyclic group substituted at the α and α′ positions, wherein R 2  may optionally be further substituted; 
 R 3  is hydrogen, halogen, —OH, —NH 2 , —CN, —R 5 , —OR 5 , —NHR 5  or —N(R 5 ) 2 ; 
 R 4  is hydrogen, halogen, —OH, —NH 2 , —CN, —R 5 , —OR 5 , —NHR 5  or —N(R 5 ) 2 ; or 
 R 3  and R 4  together with the carbon atom to which they are attached may form a 3- to 7-membered saturated or unsaturated cyclic group, wherein the cyclic group may optionally be substituted; 
 each R 5  is independently an optionally substituted C 1 -C 4  alkyl group; 
 each R 6  is independently halogen, —OH, —NO 2 , —NH 2 , —N 3 , —SH, —SO 2 H, —SO 2 NH 2 , or a saturated or unsaturated hydrocarbyl group, wherein the hydrocarbyl group may be straight-chained or branched, or be or include cyclic groups, wherein the hydrocarbyl group may optionally be substituted, and wherein the hydrocarbyl group may optionally include one or more heteroatoms N, O or S in its carbon skeleton; and 
 m is 0, 1, 2 or 3; 
 provided that any atom of L or R 1  that is directly attached to W, X, Y or Z is not the same atom of L or R 1  that is directly attached to the oxygen atom of R 1 —O-L-. 
 
       
     
     
       2. The compound or the pharmaceutically acceptable salt or solvate thereof as claimed in  claim 1 , wherein W, X, Y and Z are each independently N, NH or CH. 
     
     
       3. The compound or the pharmaceutically acceptable salt or solvate thereof as claimed in  claim 1 , wherein at least two of V, W, X, Y and Z are N or NH. 
     
     
       4. The compound or the pharmaceutically acceptable salt or solvate thereof as claimed in  claim 1 , wherein the group R 1 —O-L-, including any optional substituents, contains only atoms selected from the group consisting of carbon, hydrogen, oxygen and halogen atoms. 
     
     
       5. The compound or the pharmaceutically acceptable salt or solvate thereof as claimed in  claim 1 , wherein the group 
       
         
           
           
               
               
           
         
       
       including any optional substituents, contains from 8 to 16 atoms other than hydrogen or halogen. 
     
     
       6. The compound or the pharmaceutically acceptable salt or solvate thereof as claimed in  claim 1 , wherein each R 6  is independently selected from halo; —CN; —NO 2 ; —N 3 ; —R β ; —OH; —OR β ; —R α -halo; —R α —CN; —R α —NO 2 ; —R α —N 3 ; —R α —R β ; —R α —OH; —R α —OR β ; —SH; —SR β ; —SOR β ; —SO 2 H; —SO 2 R β ; —SO 2 NH 2 ; —SO 2 NHR β ; —SO 2 N(R β ) 2 ; —R α —SH; —R α —SR β ; —R α —SOR β ; —R α —SO 2 H; —R α —SO 2 R β ; —R α —SO 2 NH 2 ; —R α —SO 2 NHR β ; —R α —SO 2 N(R β ) 2 ; —NH 2 ; —NHR β ; —N(R β ) 2 ; —R α —NH 2 ; —R α —NHR β ; —R α —N(R β ) 2 ; —CHO; —COR β ; —COOH; —COOR β ; —OCOR β ; —R α —CHO; —R α —COR β ; —R α —COOH; —R α —COOR β ; or —R α —OCOR β ;
 wherein each —R α — is independently selected from an alkylene, alkenylene or alkynylene group, wherein the alkylene, alkenylene or alkynylene group contains from 1 to 6 atoms in its backbone, wherein one or more carbon atoms in the backbone of the alkylene, alkenylene or alkynylene group may optionally be replaced by one or more heteroatoms N, O or S, and wherein the alkylene, alkenylene or alkynylene group may optionally be substituted with one or more halo and/or —R β  groups; and 
 wherein each —R β  is independently selected from a C 1 -C 6  alkyl, C 2 -C 6  alkenyl, C 2 -C 7  alkynyl or C 3 -C 6  cyclic group, and wherein any —R β  may optionally be substituted with one or more C 1 -C 4  alkyl, C 1 -C 4  haloalkyl, C 3 -C 7  cycloalkyl, —O(C 1 -C 4  alkyl), —O(C 1 -C 4  haloalkyl), —O(C 3 -C 7  cycloalkyl), halo, —OH, —NH 2 , —CN, —C≡CH, oxo (═O), or 4- to 6-membered heterocyclic group. 
 
     
     
       7. The compound or the pharmaceutically acceptable salt or solvate thereof as claimed in  claim 1 , wherein R 2  is an aryl or a heteroaryl group, wherein the aryl or the heteroaryl group is substituted at the α and α′ positions, and wherein R 2  may optionally be further substituted. 
     
     
       8. The compound or the pharmaceutically acceptable salt or solvate thereof as claimed in  claim 7 , wherein R 2  is a fused aryl or a fused heteroaryl group, wherein a first cycloalkyl, cycloalkenyl, non-aromatic heterocyclic, aryl or heteroaryl ring is fused to the aryl or heteroaryl group across the α,β positions and a second cycloalkyl, cycloalkenyl, non-aromatic heterocyclic, aryl or heteroaryl ring is fused to the aryl or heteroaryl group across the α′,β′ positions, and wherein R 2  may optionally be further substituted. 
     
     
       9. The compound or the pharmaceutically acceptable salt or solvate thereof as claimed in  claim 1 , wherein R 2  is a cyclic group substituted at the α-position with a monovalent heterocyclic group or a monovalent aromatic group, wherein a ring atom of the heterocyclic or aromatic group is directly attached to the α-ring atom of the cyclic group, wherein the heterocyclic or aromatic group may optionally be substituted, and wherein the cyclic group is substituted at the α′-position and may optionally be further substituted. 
     
     
       10. The compound or the pharmaceutically acceptable salt or solvate thereof as claimed in  claim 1 , wherein R 3  and R 4  are hydrogen. 
     
     
       11. The compound or the pharmaceutically acceptable salt or solvate thereof as claimed in  claim 1 , wherein Q is O. 
     
     
       12. The compound or the pharmaceutically acceptable salt or solvate thereof as claimed in  claim 1 , wherein the compound is selected from the group consisting of: 
       
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
       
       and pharmaceutically acceptable salts and solvates thereof. 
     
     
       13. A pharmaceutical composition comprising the compound or the pharmaceutically acceptable salt or solvate thereof as claimed in  claim 1 , and a pharmaceutically acceptable excipient. 
     
     
       14. A method of treating, delaying onset of, or reducing risk of a disease, disorder or condition in a subject, the method comprising the step of administering an effective amount of the compound or the pharmaceutically acceptable salt or solvate thereof as claimed in  claim 1  to the subject, thereby treating, delaying onset of, or reducing risk of the disease, disorder or condition, wherein the disease, disorder or condition is responsive to NLRP3 inhibition. 
     
     
       15. The method as claimed in  claim 14 , wherein the disease, disorder or condition is selected from:
 (i) inflammation; 
 (ii) an auto-immune disease; 
 (iii) cancer; 
 (iv) an infection; 
 (v) a central nervous system disease; 
 (vi) a metabolic disease; 
 (vii) a cardiovascular disease; 
 (viii) a respiratory disease; 
 (ix) a liver disease; 
 (x) a renal disease; 
 (xi) an ocular disease; 
 (xii) a skin disease; 
 (xiii) a lymphatic condition; 
 (xiv) a psychological disorder; 
 (xv) graft versus host disease; 
 (xvi) allodynia; and 
 (xvii) any disease where an individual has been determined to carry a germline or somatic non-silent mutation in NLRP3. 
 
     
     
       16. The method as claimed in  claim 14 , wherein the disease, disorder or condition is selected from:
 (i) cryopyrin-associated periodic syndromes (CAPS); 
 (ii) Muckle-Wells syndrome (MWS); 
 (iii) familial cold autoinflammatory syndrome (FCAS); 
 (iv) neonatal onset multisystem inflammatory disease (NOMID); 
 (v) familial Mediterranean fever (FMF); 
 (vi) pyogenic arthritis, pyoderma gangrenosum and acne syndrome (PAPA); 
 (vii) hyperimmunoglobulinemia D and periodic fever syndrome (HIDS); 
 (viii) Tumour Necrosis Factor (TNF) Receptor-Associated Periodic Syndrome (TRAPS); 
 (ix) systemic juvenile idiopathic arthritis; 
 (x) adult-onset Still's disease (AOSD); 
 (xi) relapsing polychondritis; 
 (xii) Schnitzler's syndrome; 
 (xiii) Sweet's syndrome; 
 (xiv) Behcet's disease; 
 (xv) anti-synthetase syndrome; 
 (xvi) deficiency of interleukin 1 receptor antagonist (DIRA); and 
 (xvii) haploinsufficiency of A20 (HA20). 
 
     
     
       17. The method as claimed in  claim 14 , wherein the compound is administered as a pharmaceutical composition further comprising a pharmaceutically acceptable excipient. 
     
     
       18. A method of inhibiting NLRP3 in a subject, comprising administering the compound or the pharmaceutically acceptable salt or solvate thereof as claimed in  claim 1  to the subject thereby inhibiting NLRP3. 
     
     
       19. A method of analysing inhibition of NLRP3 or an effect of inhibition of NLRP3 by a compound, comprising contacting a cell or non-human animal with the compound or the pharmaceutically acceptable salt or solvate thereof as claimed in  claim 1 , and analysing inhibition of NLRP3 or an effect of inhibition of NLRP3 in the cell or non-human animal by the compound.